Results 181 to 190 of about 29,182 (218)
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Archives of Neurology, 2001
I n 1886, Jean-Martin Charcot and Pierre Marie 1,2 and Henry Tooth independently described the hereditary motor and sensory neuropathy that now bears their names. Their precise clinical description provided the foundation on which later physiological and genetic understanding of hereditary neuropathies is based.
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I n 1886, Jean-Martin Charcot and Pierre Marie 1,2 and Henry Tooth independently described the hereditary motor and sensory neuropathy that now bears their names. Their precise clinical description provided the foundation on which later physiological and genetic understanding of hereditary neuropathies is based.
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2018
Charcot-Marie-Tooth (CMT) disease is also known as hereditary motor and sensory neuropathy (HMSM) or peroneal muscular atrophy and is a group of disorders that affect peripheral nerves. The disease affects both motor and sensory peripheral nerves primarily in the lower extremities, causing sensory deficits and pain, muscle weakness, and atrophy, from ...
Patricia Dalby, Erica Coffin
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Charcot-Marie-Tooth (CMT) disease is also known as hereditary motor and sensory neuropathy (HMSM) or peroneal muscular atrophy and is a group of disorders that affect peripheral nerves. The disease affects both motor and sensory peripheral nerves primarily in the lower extremities, causing sensory deficits and pain, muscle weakness, and atrophy, from ...
Patricia Dalby, Erica Coffin
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JAMA, 1974
IT HAS been suggested that the primary abnormality in muscular dystrophy lies not in the muscle but in the motor neuron on whose trophic factor the function and survival of muscle fibers depend. 1 This "neurogenic hypothesis" 2 might explain those confusing neuropathic electromyographic responses seen in some cases of myopathy, as well as perplexing ...
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IT HAS been suggested that the primary abnormality in muscular dystrophy lies not in the muscle but in the motor neuron on whose trophic factor the function and survival of muscle fibers depend. 1 This "neurogenic hypothesis" 2 might explain those confusing neuropathic electromyographic responses seen in some cases of myopathy, as well as perplexing ...
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Charcot‐Marie‐Tooth Disease Type 2
Annals of the New York Academy of Sciences, 1999ABSTRACT: No unique genes have yet been found for CMT2, but both Cx32 and P0 appear to contribute to the phenotype. Not surprisingly, CMT2 is likely to display much more genetic heterogeneity than CMT1. However, it is also likely continue to challenge previous concepts on classification and relationship of traditional inherited phenotypes in neurology.
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2014
Charcot–Marie–Tooth disease (CMT), or hereditary peripheral neuropathy, is the most common inherited neurological disease. CMT affects both motor and sensory nerves, causing difficulty walking due to foot drop and numbness, or neuropathic pain. The subtypes of CMTs vary by nerve conduction study and inheritance patterns.
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Charcot–Marie–Tooth disease (CMT), or hereditary peripheral neuropathy, is the most common inherited neurological disease. CMT affects both motor and sensory nerves, causing difficulty walking due to foot drop and numbness, or neuropathic pain. The subtypes of CMTs vary by nerve conduction study and inheritance patterns.
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2007
Bei der heute 61-jahrigen Frau ist eine hereditare sensomotorische Neuropathie Typ 1 Charcot-Marie-Tooth seit ihrem 22. Altersjahr bekannt. Eine Schwester der Patientin leidet an der gleichen Erkrankung. Mit 38 Jahren erstmals Kontrolle durch mich wegen einer Ermudungsfraktur im rechten Mittelfusbereich. Mit orthetischen Masnahmen kann die Gehfahigkeit
R. -P. Meyer, S. Käsermann, M. Kleine
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Bei der heute 61-jahrigen Frau ist eine hereditare sensomotorische Neuropathie Typ 1 Charcot-Marie-Tooth seit ihrem 22. Altersjahr bekannt. Eine Schwester der Patientin leidet an der gleichen Erkrankung. Mit 38 Jahren erstmals Kontrolle durch mich wegen einer Ermudungsfraktur im rechten Mittelfusbereich. Mit orthetischen Masnahmen kann die Gehfahigkeit
R. -P. Meyer, S. Käsermann, M. Kleine
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Bolezen Charcot-Marie-Tooth: Charcot-Marie-Tooth disease:
2003Background. Charcot-Marie-Tooth (CMT) disease is a common inherited disorder of the peripheral nervous system. In our paper, different types of CMT are described with their typical clinical pictures, electrophysiological signs andmolecular genetic studies. CMT is classified as demyelinative and axonal type and distal motor neuronopathy.
Leonardis, Lea +2 more
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Journal of manipulative and physiological therapeutics, 1995
To discuss the similarities and differences in the clinical presentation of Charcot-Marie-Tooth Disease, an inherited peripheral neuropathy, and acquired lumbar spinal stenosis.Patients with lumbar spinal stenosis causing nerve root entrapment often have leg pain and weakness during such activities as walking or standing.
J, Martel, D, Mierau, J, Donat
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To discuss the similarities and differences in the clinical presentation of Charcot-Marie-Tooth Disease, an inherited peripheral neuropathy, and acquired lumbar spinal stenosis.Patients with lumbar spinal stenosis causing nerve root entrapment often have leg pain and weakness during such activities as walking or standing.
J, Martel, D, Mierau, J, Donat
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2017
Charcot-Marie-Tooth (CMT) disease is the most common hereditary motor and sensory neuropathic disorder. While several subtypes and inheritance patterns have been identified, the majority of cases demonstrate an autosomal dominant inheritance pattern. The pathophysiologic hallmarks of the disorder include its early and symmetric presentation involving ...
Matthew A. Varacallo +4 more
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Charcot-Marie-Tooth (CMT) disease is the most common hereditary motor and sensory neuropathic disorder. While several subtypes and inheritance patterns have been identified, the majority of cases demonstrate an autosomal dominant inheritance pattern. The pathophysiologic hallmarks of the disorder include its early and symmetric presentation involving ...
Matthew A. Varacallo +4 more
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